Good Clinical Practices (GCP's) are a set of standards and procedures which direct any clinical or investigational use of a medical product. It makes little difference if a product is being evaluated for regulatory, marketing, liability protection, outcome determination or reimbursement application. The use of the product demands clear, concise planning and documentation. At the conclusion of the trial, a company may be called upon to produce the documentation that supports their methods and materials.

Buckman Company, Inc. has more than 20 years of experience in the design, monitoring and management of clinical trials. Based on that experience, a complete Standard Operating Procedure system can be readily customized to fit any product, any study, and any company. The system is replete with Monitoring Procedures, Data Management Procedures, Monitoring Recording Forms, Audit Forms and much more.